Journal
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2014, Issue 8, Pages 1760-1765Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201301841
Keywords
Solid-phase synthesis; Acylation; Peptidomimetics; -AApeptides
Categories
Funding
- Elsa U. Pardee Foundation (USF start-up fund)
- Florida Bankhead-Coley Cancer Research Program
Ask authors/readers for more resources
Herein we report a highly efficient new method for preparing -AApeptides capable of theoretically containing any functionality; the method uses a few common N-alloc -AApeptide building blocks. More importantly, using the same approach, new classes of peptidomimetics bearing novel backbone scaffolds can also be readily generated. Our results not only demonstrate the versatility of this new synthetic method, but also highlight the possibility that the resulting novel peptidomimetics may find discrete biomedical/biomaterial applications in the future.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available